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Alternating copolymerization of carbonyl sulfide and Cyclohexene Oxide catalyzed by zinc–cobalt double metal cyanide complex

Journal 2014 · IF 3.766 · 发表于 2014 年 6 月 9 日
作者: Ming Luo,Xing-Hong Zhang,Bin-Yang Du,Qi Wang,Zhi-Qiang Fan
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摘要

This paper describes the first example of alternating copolymerization of carbonyl sulfide (COS) with cyclohexene oxide (CHO) via heterogenous catalysis of a nano-lamellar zinc–cobalt(III) double metal cyanide complex (Zn–Co(III) DMCC), providing an efficient method for converting COS to poly(cyclohexene monothiocarbonate) (PCHMTC) with an alternating degree up to 93%. The number-average molecular weight ( M n ) of PCHMTC was 6.5–25.0 kg/mol with polydispersities (PDIs) of 1.6–2.1. The productivity of the catalyst was up to 970 g polymer/g catalyst (5.0 h). The oxygen–sulfur exchange reaction (O/S ER) caused by Zn–Co(III) DMCC was largely suppressed when the reaction was performed at 100–110 °C in the presence of THF or CH 2 Cl 2 , and thus the selectivity of the monothiocarbonate over carbonate linkages was up to 98%. The mechanisms of the copolymerization and O/S ER were proposed based on the ESI-MS, GC–MS and FT-IR spectra. The obtained PCHMTC is highly transparent and exhibits good solubility in various organic solvents , high T g of 112 °C, initial decomposition temperature of 214 °C and high refractive index of 1.705.

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